Header Leaderboard Ad

Collapse

250bp reads in idba_ud

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • 250bp reads in idba_ud

    Has anyone experimented with using idba_ud on 2x250bp MiSeq data? I'm getting the following error when I tried to run it using -r and -l

    terminate called after throwing an instance of 'std::logic_error'
    what(): SequenceReader::SequenceReader() istream is invalid
    Aborted (core dumped)
    The assembler works fine when the dataset is trimmed back to 150bp. Is there some configuration that I'm missing?

  • #2
    I think 250-bp is too long to assemble at least with -r option.
    In default settings, the max is set to be 128 bp.

    To change the max value, you have to re-compile IDBA from the source as follows:

    1. change the vaue 0f 128 to 250 (or more) in /src/sequence/short_sequence.h

    static const uint32_t kMaxShortSequence = 128;
    ->
    static const uint32_t kMaxShortSequence = 250;

    2. overwrite the short_sequence.h

    3. configure & make!

    In my case, it works well with 2x250bp miseq-paired-end reads by setting 512
    Last edited by [email protected]; 04-09-2013, 02:19 AM.

    Comment


    • #3
      Thanks for the info, re-compiling IDBA with that change worked. It's strange that it doesn't work when I use the -l parameter though, isn't that the whole point of the option?

      Comment


      • #4
        I checked it under my environments.
        It seemed to be running without any errors.
        I've not changed any other points......

        Comment


        • #5
          Are you folks wokring from idba-1.1.0 or 1.0.9? I made the change above and it is altering only the max read length accepted, but not changing the maxK! When I try running it doesn't run saying my maxK is too large:

          $ idba_ud -r MiSeq_260bp.fa -o test --maxk 250


          Would either of you mind posting your full short_sequence.h files?

          Comment


          • #6
            I have been trying to run IDBA for sometimes now. I have illumina paired end reads which I merged together for testing into one file and they are 151 bases in length. I have had the same error as Kcchan and I increased the static const uint32_t kMaxShortSequence = 1600 and recompiled. It now runs till it hits k=50 and then it exits with the following error:

            kmer 50
            kmers 9815948 9845052
            merge bubble 519
            contigs: 7985 n50: 4122 max: 71069 mean: 920 total length: 7348632 n80: 919
            reads 9449880
            aligned 8473710 reads
            distance mean 229.862 sd 12592.2
            invalid insert distance
            ./command.sh: line 4: 14229 Segmentation fault /share/apps/idba-1.1.1/bin/i
            dba -r test.fa -o test_idba_out

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Improved Targeted Sequencing: A Comprehensive Guide to Amplicon Sequencing
              by seqadmin



              Amplicon sequencing is a targeted approach that allows researchers to investigate specific regions of the genome. This technique is routinely used in applications such as variant identification, clinical research, and infectious disease surveillance. The amplicon sequencing process begins by designing primers that flank the regions of interest. The DNA sequences are then amplified through PCR (typically multiplex PCR) to produce amplicons complementary to the targets. RNA targets...
              03-21-2023, 01:49 PM
            • seqadmin
              Targeted Sequencing: Choosing Between Hybridization Capture and Amplicon Sequencing
              by seqadmin




              Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches...
              03-10-2023, 05:31 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, 03-24-2023, 02:45 PM
            0 responses
            16 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 03-22-2023, 12:26 PM
            0 responses
            17 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 03-17-2023, 12:32 PM
            0 responses
            17 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 03-15-2023, 12:42 PM
            0 responses
            24 views
            0 likes
            Last Post seqadmin  
            Working...
            X